Optic atrophy and cataract, autosomal dominant Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537128
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Genes

1 genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) 2.88009